NEOMED ORAL/ENTERAL SYRINGE— 510(k) K122373
Substantially EquivalentNeomed, Inc.
FDA 510(k) clearance K122373 for NEOMED ORAL/ENTERAL SYRINGE, Substantially Equivalent on 2012-09-20. Applicant: Neomed, Inc.. Device class: 2.
Clearance details
- Applicant
- Neomed, Inc.
- Product code
- Code FMF
- Device class
- Class 2
- Regulation
- 21 CFR 880.5860
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Woodstock, GA, US
Recent devices under product code FMF
view allMore clearances from Neomed, Inc.
view all- K183540 — Oral/Enteral Syringes with ENFit connector (12 mL to 60 mL), Low Dose Tip Oral/Enteral Syringes with ENFit connector (1 mL to 6 mL)
- K161039 — NeoConnect Oral/Enteral Syringes with ENFit connector (12 mL to 100 mL) and NeoConnect Low Dose Tip Oral/Enteral Syringes with ENFit connector (0.5 mL to 6mL)
- K152857 — NeoMed NeoConnect Enteral Syringes with ENFit Connector and compatible NeoSecure Tip Caps
- K143344 — NeoMed NeoConnect Enteral Syringes with ENFit Connector
- K120182 — NEOMED GASTROINTESTINAL TUBE AND ACCESSORIES
Adverse events under product code FMF
product code FMF- Death
- 15
- Injury
- 2,263
- Malfunction
- 29,722
- Other
- 17
- Total
- 32,017
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.